Tarantino P - Search Results

1

No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.

Mumoli L, Tarantino P, Michelucci R, Bianchi A, Labate A, Franceschetti S, Marini C, Striano P, Gagliardi M, Ferlazzo E, Sofia V, Pennese L, Annesi G, Aguglia U, Guerrini R, Zara F, Gambardella A; Genetic Commission, Italian League Against Epilepsy. Mumoli L, et al. Among authors: tarantino p. Epilepsia. 2015 Apr;56(4):e40-3. doi: 10.1111/epi.12944. Epub 2015 Mar 6. Epilepsia. 2015. PMID: 25752200 Free article.

2

Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences.

Labate A, Tarantino P, Viri M, Mumoli L, Gagliardi M, Romeo A, Zara F, Annesi G, Gambardella A. Labate A, et al. Among authors: tarantino p. Epilepsia. 2012 Dec;53(12):e196-9. doi: 10.1111/epi.12009. Epub 2012 Nov 5. Epilepsia. 2012. PMID: 23126439 Free article.

3

Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP.

Labate A, Tarantino P, Palamara G, Gagliardi M, Cavalcanti F, Ferlazzo E, Sturniolo M, Incorpora G, Annesi G, Aguglia U, Gambardella A. Labate A, et al. Among authors: tarantino p. Epilepsy Res. 2013 May;104(3):280-4. doi: 10.1016/j.eplepsyres.2012.10.014. Epub 2013 Jan 23. Epilepsy Res. 2013. PMID: 23352743

4

PCDH19 mutations in female patients from Southern Italy.

Gagliardi M, Annesi G, Sesta M, Tarantino P, Conti P, Labate A, Di Rosa G, Quattrone A, Gambardella A. Gagliardi M, et al. Among authors: tarantino p. Seizure. 2015 Jan;24:118-20. doi: 10.1016/j.seizure.2014.08.010. Epub 2014 Aug 30. Seizure. 2015. PMID: 25218114 Free article.

5

Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus.

Annesi G, Gambardella A, Carrideo S, Incorpora G, Labate A, Pasqua AA, Civitelli D, Polizzi A, Annesi F, Spadafora P, Tarantino P, Cirò Candiano IC, Romeo N, De Marco EV, Ventura P, LePiane E, Zappia M, Aguglia U, Pavone L, Quattrone A. Annesi G, et al. Among authors: tarantino p. Epilepsia. 2003 Sep;44(9):1257-8. doi: 10.1046/j.1528-1157.2003.22503.x. Epilepsia. 2003. PMID: 12919402 Free article. No abstract available.

6

Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy.

De Marco EV, Gambardella A, Annesi F, Labate A, Carrideo S, Forabosco P, Civitelli D, Candiano IC, Tarantino P, Annesi G, Quattrone A. De Marco EV, et al. Among authors: tarantino p. Epilepsy Res. 2007 Apr;74(1):70-3. doi: 10.1016/j.eplepsyres.2006.12.006. Epub 2007 Feb 26. Epilepsy Res. 2007. PMID: 17324557

7

Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine.

Cestèle S, Labate A, Rusconi R, Tarantino P, Mumoli L, Franceschetti S, Annesi G, Mantegazza M, Gambardella A. Cestèle S, et al. Among authors: tarantino p. Epilepsia. 2013 May;54(5):927-35. doi: 10.1111/epi.12123. Epub 2013 Feb 8. Epilepsia. 2013. PMID: 23398611 Free article. Review.

8

Frequency of the ASP620ASN mutation in VPS35 and Arg1205His mutation in EIF4G1 in familial Parkinson's disease from South Italy.

Gagliardi M, Annesi G, Tarantino P, Nicoletti G, Quattrone A. Gagliardi M, et al. Among authors: tarantino p. Neurobiol Aging. 2014 Oct;35(10):2422.e1-2. doi: 10.1016/j.neurobiolaging.2014.04.020. Epub 2014 Apr 26. Neurobiol Aging. 2014. PMID: 24854799

9

A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification.

Gagliardi M, Morelli M, Annesi G, Nicoletti G, Perrotta P, Pustorino G, Iannello G, Tarantino P, Gambardella A, Quattrone A. Gagliardi M, et al. Among authors: tarantino p. Gene. 2015 Aug 15;568(1):109-11. doi: 10.1016/j.gene.2015.05.005. Epub 2015 May 7. Gene. 2015. PMID: 25958344

10

Role of G-protein coupled receptor kinase 5 gene in cognitive impairment in Parkinson's disease.

Nicoletti G, De Luca V, Tarantino P, Gagliardi M, Iannello G, Novellino F, Morelli M, Annesi G, Quattrone A. Nicoletti G, et al. Among authors: tarantino p. Psychiatry Res. 2015 Dec 30;230(3):975-7. doi: 10.1016/j.psychres.2015.11.026. Epub 2015 Nov 17. Psychiatry Res. 2015. PMID: 26614013

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